Chemically Defined Antibodyâ and Small Molecule ... - ACS Publications

Subscriber access provided by READING UNIV

Communication

Chemically-defined antibody- and small molecule-drug conjugates for in vivo tumor targeting applications: a comparative analysis Samuele Cazzamalli, Alberto Dal Corso, Fontaine Widmayer, and Dario Neri J. Am. Chem. Soc., Just Accepted Manuscript • DOI: 10.1021/jacs.7b13361 • Publication Date (Web): 17 Jan 2018 Downloaded from http://pubs.acs.org on January 17, 2018

Just Accepted “Just Accepted” manuscripts have been peer-reviewed and accepted for publication. They are posted online prior to technical editing, formatting for publication and author proofing. The American Chemical Society provides “Just Accepted” as a free service to the research community to expedite the dissemination of scientific material as soon as possible after acceptance. “Just Accepted” manuscripts appear in full in PDF format accompanied by an HTML abstract. “Just Accepted” manuscripts have been fully peer reviewed, but should not be considered the official version of record. They are accessible to all readers and citable by the Digital Object Identifier (DOI®). “Just Accepted” is an optional service offered to authors. Therefore, the “Just Accepted” Web site may not include all articles that will be published in the journal. After a manuscript is technically edited and formatted, it will be removed from the “Just Accepted” Web site and published as an ASAP article. Note that technical editing may introduce minor changes to the manuscript text and/or graphics which could affect content, and all legal disclaimers and ethical guidelines that apply to the journal pertain. ACS cannot be held responsible for errors or consequences arising from the use of information contained in these “Just Accepted” manuscripts.

Journal of the American Chemical Society is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society. Copyright © American Chemical Society. However, no copyright claim is made to original U.S. Government works, or works produced by employees of any Commonwealth realm Crown government in the course of their duties.

Page 1 of 11 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Journal of the American Chemical Society

Chemically-defined antibody- and small molecule-drug conjugates for in vivo tumor targeting applications: a comparative analysis Samuele Cazzamalli, Alberto Dal Corso, Fontaine Widmayer and Dario Neri* Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology (ETH Zürich), Vladimir-PrelogWeg 4, CH-8093 Zurich (Switzerland) Supporting Information Placeholder ABSTRACT: We present the first direct comparative

evaluation of an antibody-drug conjugate and of a small molecule-drug conjugate for cancer therapy, using chemically-defined products which bind with highaffinity to carbonic anhydrase IX, a marker of tumor hypoxia and of renal cell carcinoma.

Conventional cancer chemotherapeutic agents do not preferentially localize at the tumor site.1-4 This pharmacokinetic limitation often contributes to the onset of toxicity and prevents dose escalation to therapeutically-active regimens.5 In an attempt to improve the therapeutic index of cancer chemotherapy, monoclonal antibodies and small organic ligands have been proposed as delivery vehicles of cytotoxic compounds, allowing the construction of antibody-drug conjugates (ADCs)68 and small molecule-drug conjugates (SMDCs).9 Four ADC products have gained marketing authorization for cancer therapy10-14, while SMDCs are still under investigation in clinical trials.15 Monoclonal antibodies can recognize their molecular target with exquisite specificity, but their penetration into solid tumor masses can be suboptimal.16 ADCs have high cost-of-goods and their long circulatory halflife may cause premature drug release.17,18 While antibodies can be routinely generated against virtually any protein antigen19, the isolation of small organic ligands is more difficult and SMDC applications have so far been limited to a small number of targets (e.g. Folate Receptor, Prostate-Specific Membrane Antigen, Somatostatin Receptors and Carbonic Anhydrase IX).20-23 In principle, peptides could also be considered as ligands for pharmacodelivery applications, provided that they display acceptably low kidney uptake values.22,24 Here we report the first comparative analysis of two chemically-defined ADC and SMDC products, directed

against the same molecular target. Carbonic anhydrase IX (CAIX) is a cell membrane-protein overexpressed in tumor hypoxia and in certain malignancies, including renal cell carcinoma, colorectal, urothelial, lung, stomach, pancreas, breast, head and neck, ovaries, brain and cervix cancer.25,26 CAIX is membrane protein which has been targeted in clinical trials with radionuclide conjugates27,28 and with an ADC product.29 A growing body of evidence indicates that ADCs and SMDCs can be efficacious even in the absence of ligand internalization, if drugs are efficiently released within the tumor mass by a number of different extracellular proteases or by the reduction of disulfide linkers.30-37 Indeed, experimental evidence from various laboratories indicates that CAIX does not efficiently internalize upon ligand binding.23,34,38 For the development of an ADC product against CAIX, we used a high-affinity monoclonal antibody, isolated from a phage display library [Supporting Information]. The SMDC product was based on an acetazolamide derivative with sub-nanomolar dissociation constant to CAIX, recently isolated from a DNAencoded chemical library.39 For both agents, we used the linker-payload of Adcetris™, an approved ADC product40,41, featuring a cleavable Val-Cit dipeptide, a self-immolating spacer and monomethyl auristatin E (MMAE) as cytotoxic drug [Figure 1]. In order to generate chemically defined products with drugantibody ratio (DAR) of 2, antibodies were used in human IgG1 format, in which three cysteine residues in the hinge region had been mutated to serines, thus permitting a site-specific coupling with maleimido derivatives42,43 [Figure 1]. The SMDCs featured a drugligand ratio (DLR) of 1.

ACS Paragon Plus Environment

Journal of the American Chemical Society 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 2 of 11

The BIAcore methodology may under-estimate KD values for antibodies in homobivalent IgG format against bivalent antigens (due to a chelate binding mode) and to overestimate KD values for small organic ligands with very high kon, due to limitation of diffusion speed within the microsensor chip hydrogel.

Figure 1. Chemical structures and biochemical characterization of anti-CAIX ADC and SMDC products. Ligandlinker-payload structures, as well as the site of conjugation are indicated. Size exclusion chromatography profile and SDS-PAGE relative to the CAIX-specific ADC(+) product. Lanes NR and R represent the final ADC in nonreducing and reducing conditions, respectively. SPR analysis of ADC(+) and the negative control ADC(-) for their binding to recombinant human CAIX. Sensograms are referred to different concentration of the conjugates. Liquid chromatography and mass spectrometry analysis of SMDC(+). SPR sensorgrams of a serial dilution of SMDC(+) and SMDC(-) against recombinant human CAIX. Fitting of sensorgrams related to ADC(+) and SMDC(+) allowed calculation of the corresponding apparent binding constants: kon,SMDC(+) = 3.4 105 M-1s-1, koff,SMDC(+) = 3.4 10-3 s-1, KD,SMDC(+) = 10 nM; kon,ADC(+) = 1.7 105 M-1s-1, koff,ADC(+) = 2.2 10-5 s-1, KD,ADC(+) = 0.13 nM.

Methodologies to assess product purity and identity included SDS-PAGE analysis, gel-filtration and mass spectrometry for the ADCs, while the SMDCs were characterized by UPLC and mass spectrometry. Binding to the cognate CAIX antigen was studied by BIAcore analysis [Figure 1 + Supporting Information]. Two structurally-related compounds were used as negative controls, as they featured ligands of irrelevant specificity in the mouse. The KSF antibody, specific to hen egg lysozyme, was used to generate an ADC product [ADC(-)], using an identical immunoglobulin format as for the anti-CAIX agent. Omission of the acetazolamide moiety in the small ligand structure led to a drug conjugate [SMDC(-)], devoid of any detectable CAIX binding [Figure 1 + Supporting Information]. In order to assess the tumor-homing properties of the anti-CAIX antibody and small organic ligands, two experimental methodologies were used. Radiolabeled preparations were administered intravenously to mice bearing subcutaneous SKRC-52 tumors and the percent of injected dose per gram (%ID/g) was assessed by organ counting at relevant time points. The anti-CAIX antibody exhibited an unfavorable tumor/blood distribution ratio 48 hours after the injection, while the small organic ligand showed a substantially higher tumor uptake (~40% ID/g) and a tumor/blood distribution ratio of ~100:1 [Figure 2A + Supporting Information]. The results obtained with AAZ+ were clearly superior to the ones obtained with monovalent acetazolamide or with homobivalent acetazolamide derivatives.33,44 In a second experiment, the two anti-CAIX agents were administered to tumor-bearing mice and the relative uptake in relevant organs was assessed by fluorescence microscopy procedures [Figure 2B]. Twenty-four hours after administration, the antibody exhibited a patchy perivascular uptake in tumor cells, similar to what had previously been reported for trastuzumab in breast cancer models16, while the small organic ligand exhibited a homogenous uptake in the neoplastic mass already after 1 hour (targeting results are shown at different time points, since the antibody clears much more slowly from circulation). The antiCAIX antibody exhibited an undesired targeting of heart tissue, while the small ligand had a residual accumulation in kidney and lung. The results obtained with radioactive and fluorescence detection were in good agreement [Figure 2B + Supporting Information].


Page 3 of 11 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


Figure 2. Evaluation of the tumor-targeting performance of the anti-CAIX XE114 antibody (mAb+) and the small ligand AAZ+ (SM+) against human renal cell carcinoma cells SKRC-52 xenografted in mice. (A) Quantification of ligand uptake in tumor and blood after administration of radiolabeled preparations of IgG(XE114) (mAb+) and of a radiolabeled derivative of AAZ+ (SM+). Microscopic distribution of IgG(XE114) (mAb+) and of a fluorescently labeled derivative of AAZ+ (SM+) in SKRC-52 tumors (B) and in healthy organs (C) after IV administration. Images related to mAb+ and SM+ products were taken 24 hours and 1 hour post injection, respectively. mAb- and SM- relate to the corresponding negative controls. Green = Ligand (mAb+ or SM+); Blue = DAPI staining. Scale bar = 100 µm.

Therapy experiments were performed at equimolar doses of cytotoxic agent in nude mice bearing human SKRC-52 tumors, a subcutaneous xenograft model of kidney cancer that does not efficiently metastasize in vivo after implantation. The SMDC products were ad-

ministered at 250 nmol/Kg, while ADCs were injected at 125 nmol/Kg, as they featured a DAR of 2 [Figure 3]. Tumors grew rapidly in mice treated with saline. The CAIX-targeted SMDC product [SMDC(+)] exhibited a potent tumor-growth retardation, while the nega-



Page 4 of 11

tive control counterpart did not slow down tumor growth. ADC(+) was potently active in this cancer model, but (like the SMDC product) did not result in complete tumor eradication. Moreover, the difference in activity between positive- and negative-control ADCs was minimal. All treatments were well tolerated, even though ADC(+) led to a transient loss of 5% body weight.

the small CAIX ligand exhibited an efficient and homogenous targeting of the neoplastic mass. However, small ligands (including the one used in this study) are often efficiently filtered via the renal route and may display an undesired uptake in the kidney interstitium. A residual uptake of the CAIX ligand in stomach and lung was observed at early time points, but its magnitude was substantially lower compared to the one in tumors [Supporting Information]. The SMDC product exhibited an excellent discrimination, relative to its negative control counterpart, both in biodistribution and in therapy studies. However, the therapeutic activity was slightly inferior compared to the ADC. This observation was somewhat unexpected, in light of the biodistribution results of Figure 2. It is likely that the anti-CAIX ADC product displays its activity mainly by a slow release of the highly-potent MMAE cytotoxic payload, as a strong anti-cancer activity was also observed for the anti-lysozyme ADC(-) negative control. Interestingly, charged analogues of MMAE do not exhibit comparable therapeutic activity in vivo, when coupled to non-internalizing ligands.47 The Val-Cit-based linker-payload combination used in this study is the same as the one used in the clinically-approved Adcetris™ ADC product. It is possible that the SMDC agent may benefit from a careful tuning of the velocity of payload release.48 Considering that the high-affinity acetazolamide-based CAIX ligand described in this article displays a tumor/blood distribution ratio of ~100:1 six hours after i.v. injection, a more labile linker may increase the rate of tumor cell damage and may therefore be more active. An interplay between dose rate and therapeutic activity has previously been reported for radionuclide-based therapeutics.49,50 It also remains to be seen whether ADCs and SMDCs still exhibit a comparable therapeutic activity, when those products are directed against a target which internalizes well.

Figure 3. Comparative therapeutic analysis of anti-CAIX antibody-drug conjugate ADC(+) and small moleculedrug conjugate SMDC(+) in BALB/c nu/nu mice bearing SKRC-52 xenografts. In the experiment, ADC(-) and SMDC(-) derivatives devoid of the targeting moieties were used as negative controls. (A) Changes in tumor volume for different treatment groups. (B) Body weight changes experienced by the animals during the therapy experiment. The arrows indicate intravenous (i.v.) administration of the corresponding agent. DLR = drug-ligand ratio; DAR = drug-antibody ratio.

ASSOCIATED CONTENT

The experiments indicate that both ADC and SMDC products can mediate a potent anti-tumor effect in tumor-bearing mice, when used at the same molar dose. The main limitations for ADC technology may be associated with a sub-optimal tumor uptake, essentially limited to perivascular cancer cells.16,45,46 By contrast,

The Supporting Information is available free of charge on the ACS Publications website. Detailed experimental procedures and Supplementary Figures (PDF)

AUTHOR INFORMATION Corresponding Author

*[email protected] Notes D.N. is a co-founder and shareholder of Philogen (www.philogen.com), a Swiss-Italian Biotech company that operates in the field of ligand-based pharmacodelivery.

ACKNOWLEDGMENT


Page 5 of 11 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


The authors gratefully acknowledge financial support from ETH Zürich, the Swiss National Science Foundation (Project Nr. 310030B_163479/1 and SINERGIA CRSII2_160699/1), ERC Advanced Grant “Zauberkugel” (670603) and Kommission für Technologie und Innovation (Grant Nr. 17072.1). D.N. and A.D.C. acknowledge the Novartis Foundation for medical–biological Research for financial support.

REFERENCES (1) Bosslet, K.; Straub, R.; Blumrich, M.; Czech, J.; Gerken, M.; Sperker, B.; Kroemer, H. K.; Gesson, J. P.; Koch, M.; Monneret, C. Cancer Res. 1998, 58, 1195-201. (2) Cao, Q.; Li, Z. B.; Chen, K.; Wu, Z.; He, L.; Neamati, N.; Chen, X. Eur. J. Nucl. Med. Mol. Imaging 2008, 35, 1489-1498. (3) van der Veldt, A. A.; Lubberink, M.; Mathijssen, R. H.; Loos, W. J.; Herder, G. J.; Greuter, H. N.; Comans, E. F.; Rutten, H. B.; Eriksson, J.; Windhorst, A. D.; Hendrikse, N. H.; Postmus, P. E.; Smit, E. F.; Lammertsma, A. A. Clin. Cancer Res. 2013, 19, 41634173. (4) van der Veldt, A. A.; Hendrikse, N. H.; Smit, E. F.; Mooijer, M. P.; Rijnders, A. Y.; Gerritsen, W. R.; van der Hoeven, J. J.; Windhorst, A. D.; Lammertsma, A. A.; Lubberink, M. Eur. J. Nucl. Med. Mol. Imaging 2010, 37, 1950-1958. (5) Van Cutsem, E.; Moiseyenko, V. M.; Tjulandin, S.; Majlis, A.; Constenla, M.; Boni, C.; Rodrigues, A.; Fodor, M.; Chao, Y.; Voznyi, E.; Risse, M. L.; Ajani, J. A.; Group, V. S. J. Clin. Oncol. 2006, 24, 4991-4997. (6) Chari, R. V.; Miller, M. L.; Widdison, W. C. Angew. Chem. Int. Ed. 2014, 53, 3796-3827. (7) Senter, P. D. Curr. Opin. Chem. Biol. 2009, 13, 235-244. (8) Gerber, H. P.; Koehn, F. E.; Abraham, R. T. Nat. Prod. Rep. 2013, 30, 625-639. (9) Krall, N.; Scheuermann, J.; Neri, D. Angew. Chem. Int. Ed. 2013, 52, 1384-402. (10) Lamb, Y. N. Drugs 2017, 77, 1603-1610. (11) Sassoon, I.; Blanc, V. Methods Mol. Biol. 2013, 1045, 1-27. (12) Burris, H. A. Am. Soc. Clin. Oncol. Educ. Book 2013, doi: 10.1200/EdBook_AM.2013.33.e99. (13) Tvito, A.; Rowe, J. M. Expert Opin. Biol. Ther. 2017, 17, 1557-1564. (14) Appelbaum, F. R.; Bernstein, I. D. Blood 2017, 130, 23732376. (15) Srinivasarao, M.; Galliford, C. V.; Low, P. S. Nat. Rev. Drug. Discov. 2015, 14, 203-219. (16) Dennis, M. S.; Jin, H.; Dugger, D.; Yang, R.; McFarland, L.; Ogasawara, A.; Williams, S.; Cole, M. J.; Ross, S.; Schwall, R. Cancer Res. 2007, 67, 254-261. (17) Giles, F. J.; Kantarjian, H. M.; Kornblau, S. M.; Thomas, D. A.; Garcia-Manero, G.; Waddelow, T. A.; David, C. L.; Phan, A. T.; Colburn, D. E.; Rashid, A.; Estey, E. H. Cancer 2001, 92, 406-413. (18) Rajvanshi, P.; Shulman, H. M.; Sievers, E. L.; McDonald, G. B. Blood 2002, 99, 2310-2314. (19) Winter, G.; Griffiths, A. D.; Hawkins, R. E.; Hoogenboom, H. R. Annu. Rev. Immunol. 1994, 12, 433-455. (20) Low, P. S.; Henne, W. A.; Doorneweerd, D. D. Acc. Chem. Res. 2008, 41, 120-129. (21) Hillier, S. M.; Maresca, K. P.; Lu, G.; Merkin, R. D.; Marquis, J. C.; Zimmerman, C. N.; Eckelman, W. C.; Joyal, J. L.; Babich, J. W. J. Nucl. Med. 2013, 54, 1369-1376.

(22) Ginj, M.; Zhang, H.; Waser, B.; Cescato, R.; Wild, D.; Wang, X.; Erchegyi, J.; Rivier, J.; Macke, H. R.; Reubi, J. C. Proc. Natl. Acad. Sci. U S A 2006, 103, 16436-16441. (23) Krall, N.; Pretto, F.; Decurtins, W.; Bernardes, G. J.; Supuran, C. T.; Neri, D. Angew. Chem. Int. Ed. 2014, 53, 4231-4235. (24) Wang, S.; Placzek, W.J.; Stebbins, J.L.; Mitra, S., Noberini, R.; Koolpe, M.; Zhang, Z.; Dahl, R.; Pasquale, E.B.; Pellecchia, M. J. Med. Chem. 2012, 55, 2427-2436. (25) Pastorekova, S.; Parkkila, S.; Pastorek, J.; Supuran, C. T. J. Enzyme Inhib. Med. Chem. 2004, 19, 199-229. (26) Lv, P. C.; Roy, J.; Putt, K. S.; Low, P. S. Mol. Cancer Ther. 2017, 16, 453-460. (27) Chrastina, A.; Zavada, J.; Parkkila, S.; Kaluz, S.; Kaluzova, M.; Rajcani, J.; Pastorek, J.; Pastorekova, S. Int. J. Cancer 2003, 105, 873-881. (28) van Schaijk, F. G.; Oosterwijk, E.; Molkenboer-Kuenen, J. D.; Soede, A. C.; McBride, B. J.; Goldenberg, D. M.; Oyen, W. J.; Corstens, F. H.; Boerman, O. C. J. Nucl. Med. 2005, 46, 495-501. (29) Petrul, H. M.; Schatz, C. A.; Kopitz, C. C.; Adnane, L.; McCabe, T. J.; Trail, P.; Ha, S.; Chang, Y. S.; Voznesensky, A.; Ranges, G.; Tamburini, P. P. Mol. Cancer Ther. 2012, 11, 340-349. (30) Bernardes, G. J.; Casi, G.; Trussel, S.; Hartmann, I.; Schwager, K.; Scheuermann, J.; Neri, D. Angew. Chem. Int. Ed. 2012, 51, 941944. (31) Perrino, E.; Steiner, M.; Krall, N.; Bernardes, G. J.; Pretto, F.; Casi, G.; Neri, D. Cancer Res. 2014, 74, 2569-2578. (32) Dal Corso, A.; Cazzamalli, S.; Gébleux, R.; Mattarella, M.; Neri, D. Bioconjugate Chem. 2017, 28, 1826-1833. (33) Krall, N.; Pretto, F.; Neri, D. Chem. Sci. 2014, 5, 3640-3644. (34) Cazzamalli, S.; Dal Corso, A.; Neri, D. Mol. Cancer Ther. 2016, 15, 2926-2935. (35) Caculitan, N. G.; Dela Cruz Chuh, J.; Ma, Y.; Zhang, D.; Kozak, K. R.; Liu, Y.; Pillow, T. H.; Sadowsky, J.; Cheung, T. K.; Phung, Q.; Haley, B.; Lee, B. C.; Akita, R. W.; Sliwkowski, M. X.; Polson, A. G. Cancer Res. 2017, 77, 7027-7037. (36) Dorywalska, M.; Dushin, R.; Moine, L.; Farias, S. E.; Zhou, D.; Navaratnam, T.; Lui, V.; Hasa-Moreno, A.; Casas, M. G.; Tran, T. T.; Delaria, K.; Liu, S. H.; Foletti, D.; O'Donnell, C. J.; Pons, J.; Shelton, D. L.; Rajpal, A.; Strop, P. Mol. Cancer Ther. 2016, 15, 958-970. (37) Freedy, A. M.; Matos, M. J.; Boutureira, O.; Corzana, F.; Guerreiro, A.; Akkapeddi, P.; Somovilla, V. J.; Rodrigues, T.; Nicholls, K.; Xie, B.; Jimenez-Oses, G.; Brindle, K. M.; Neves, A. A.; Bernardes, G. J. L. J. Am. Chem. Soc. 2017, 139, 18365-18375. (38) Lv, P. C.; Putt, K. S.; Low, P. S. Bioconjugate Chem. 2016, 27, 1762-1769. (39) Wichert, M.; Krall, N.; Decurtins, W.; Franzini, R. M.; Pretto, F.; Schneider, P.; Neri, D.; Scheuermann, J. Nat. Chem. 2015, 7, 241-249. (40) Fanale, M. A. Lancet Oncol. 2017, 18, 1566-1568. (41) Pro, B.; Advani, R.; Brice, P.; Bartlett, N. L.; Rosenblatt, J. D.; Illidge, T.; Matous, J.; Ramchandren, R.; Fanale, M.; Connors, J. M.; Fenton, K.; Huebner, D.; Pinelli, J. M.; Kennedy, D. A.; Shustov, A. Blood 2017, 130, 2709-17. (42) McDonagh, C. F.; Turcott, E.; Westendorf, L.; Webster, J. B.; Alley, S. C.; Kim, K.; Andreyka, J.; Stone, I.; Hamblett, K. J.; Francisco, J. A.; Carter, P. Protein Eng. Des. Sel. 2006, 19, 299307. (43) Gébleux, R.; Stringhini, M.; Casanova, R.; Soltermann, A.; Neri, D. Int. J. Cancer 2017, 140, 1670-1679. (44) Krall, N.; Pretto, F.; Mattarella, M.; Müller, C.; Neri, D. J. Nucl. Med. 2016, 57, 943-949.



(45) Saga, T.; Neumann, R. D.; Heya, T.; Sato, J.; Kinuya, S.; Le, N.; Paik, C. H.; Weinstein, J. N. Proc. Natl. Acad. Sci. U S A 1995, 92, 8999-9003. (46) Adams, G. P.; Schier, R.; McCall, A. M.; Simmons, H. H.; Horak, E. M.; Alpaugh, R. K.; Marks, J. D.; Weiner, L. M. Cancer Res. 2001, 61, 4750-4755. (47) Dal Corso, A.; Gébleux, R.; Murer, P.; Soltermann, A.; Neri, D. J. Control. Release 2017, 264, 211-218.

Page 6 of 11

(48) Cazzamalli, S.; Dal Corso, A.; Neri, D. J. Control. Release 2017, 246, 39-45. (49) Kratochwil, C.; Bruchertseifer, F.; Rathke, H.; Bronzel, M.; Apostolidis, C.; Weichert, W.; Haberkorn, U.; Giesel, F. L.; Morgenstern, A. J. Nucl. Med. 2017, 58, 1624-1631. (50) Kratochwil, C.; Bruchertseifer, F.; Giesel, F. L.; Weis, M.; Verburg, F. A.; Mottaghy, F.; Kopka, K.; Apostolidis, C.; Haberkorn, U.; Morgenstern, A. J. Nucl. Med. 2016, 57, 1941-1944.


Page 7 of 11 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


Table of Content


7


Figure 1. Chemical structures and biochemical characterization of anti-CAIX ADC and SMDC products. Ligand-linker-payload structures, as well as the site of conjugation are indicated. Size exclusion chromatography profile and SDS-PAGE relative to the CAIX-specific ADC(+) product. Lanes NR and R represent the final ADC in non-reducing and reducing conditions, respectively. SPR analysis of ADC(+) and the negative control ADC(-) for their binding to recombinant human CAIX. Sensograms are referred to different concentration of the conjugates. Liquid chromatography and mass spectrometry analysis of SMDC(+). SPR sensorgrams of a serial dilution of SMDC(+) and SMDC(-) against recombinant human CAIX. Fitting of sensorgrams related to ADC(+) and SMDC(+) allowed calculation of the corresponding apparent binding constants: kon,SMDC(+) = 3.4 105 M-1s-1, koff,SMDC(+) = 3.4 10-3 s-1, KD,SMDC(+) = 10 nM; kon,ADC(+) = 1.7 105 M-1s-1, koff,ADC(+) = 2.2 10-5 s-1, KD,ADC(+) = 0.13 nM. The BIAcore methodology may under-estimate KD values for antibodies in homobivalent IgG format against bivalent antigens (due to a chelate binding mode) and to over-estimate KD values for small organic ligands with very high kon, due to limitation of diffusion speed within the microsensor chip hydrogel.


Page 8 of 11

Page 9 of 11 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


83x167mm (300 x 300 DPI)



Figure 2. Evaluation of the tumor-targeting performance of the anti-CAIX XE114 antibody (mAb+) and the small ligand AAZ+ (SM+) against human renal cell carcinoma cells SKRC-52 xenografted in mice. (A) Quantification of ligand uptake in tumor and blood after administration of radiolabeled preparations of IgG(XE114) (mAb+) and of a radiolabeled derivative of AAZ+ (SM+). Microscopic distribution of IgG(XE114) (mAb+) and of a fluorescently labeled derivative of AAZ+ (SM+) in SKRC-52 tumors (B) and in healthy organs (C) after IV administration. Images related to mAb+ and SM+ products were taken 24 hours and 1 hour post injection, respectively. mAb- and SM- relate to the corresponding negative controls. Green = Ligand (mAb+ or SM+); Blue = DAPI staining. Scale bar = 100 µm. 162x168mm (300 x 300 DPI)


Page 10 of 11

Page 11 of 11 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


Figure 3. Comparative therapeutic analysis of anti-CAIX antibody-drug conjugate ADC(+) and small molecule-drug conjugate SMDC(+) in BALB/c nu/nu mice bearing SKRC-52 xenografts. In the experiment, ADC(-) and SMDC(-) derivatives devoid of the targeting moieties were used as negative controls. (A) Changes in tumor volume for different treatment groups. (B) Body weight changes experienced by the animals during the therapy experiment. The arrows indicate intravenous (i.v.) administration of the corresponding agent. DLR = drug-ligand ratio; DAR = drug-antibody ratio. 79x123mm (300 x 300 DPI)



Table of Content 45x44mm (600 x 600 DPI)


Page 12 of 11

Chemically Defined Antibodyâ and Small Molecule ... - ACS Publications

Recommend Documents

Chemically Defined Antibodyâ and Small Molecule ... - ACS Publications